Senior Clinical Research Coordinator
Description
Job Duties
- Coordinate the day-to-day clinical operations of clinical research studies
- Perform study procedures in accordance with GCP and study protocols
- Organize and maintain paper and electronic study data in a complete and correct manner
- Work closely with recruitment and prescreening teams to meet study enrollment goals
- Conduct diagnostic, efficacy, and safety assessments as needed
- Mentor and lead less experienced coordinators and/or research assistants
- Take ownership of team productivity (enrollment) and quality metrics
- Own study study start-up tasks, including vendor communication and qualification
Job Requirements
- Five (5) or more years of industry-sponsored drug trial experience
- Demonstrated ability to work on high-enrolling Phase II/III clinical trials
- Attention to detail and the ability to handle multiple tasks with precision
- Demonstrated ability to work accurately and quickly with CTMS
- A command of professional spoken and written English
Skills
As published by lever · 1 question · 1 written answer
Which location are you applying for?, Resume/CV, Full name, Email, Phone, Current location, Current company, LinkedIn URL
- Please provide details about your clinical trial experience. optional